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  4. NDC Product Code: 70758-100 Repiel Perfect Fit Mask Firming

NDC 70758-100 Repiel Perfect Fit Mask Firming

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70758-100?
  4. Repiel Perfect Fit Mask Firming Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70758-100
Proprietary Name:
Repiel Perfect Fit Mask Firming
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Cosrise Co.,ltd
Labeler Code:
70758
Product Label ID:
f0b13fb0-c9a7-4f27-ab05-b7e07aa87a5e
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 70758-100?

The NDC code 70758-100 is assigned by the FDA to the product Repiel Perfect Fit Mask Firming which is product labeled by The Cosrise Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70758-100-02 10 pouch in 1 carton / 25 ml in 1 pouch (70758-100-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Repiel Perfect Fit Mask Firming?

Indications & Usage: Get rid of saggy, younger looking skin. 1. Wash and cleanse the face to increase the effect of the mask 2. After removing mesh, apply the mask sheet smoothly to your face removing the fabric layer 3. Relax leaving the mask on, After 15~20 minute, peel away mask. Massage gently to maximize the effect of essence

Which are Repiel Perfect Fit Mask Firming UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Repiel Perfect Fit Mask Firming Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".